| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36990208-36990311 | Common:3; Rare:39; Clinvar (benign):3 | ||||
| chr21:37072575-37072746 | Common:5; Rare:86 | ||||
| chr21:37072998-37073434 | Common:5; Rare:157 | ||||
| chr21:37267289-37267596 | Common:3; Rare:108 | ||||
| chr21:37267679-37267698 | Rare:7 | ||||
| chr21:37267876-37268028 | Rare:45 | ||||
| chr21:37365884-37366112 | Rare:69 | ||||
| chr21:37366695-37366794 | Rare:31 | ||||
| chr21:38498451-38498748 | Common:1; Rare:42 | ||||
| chr21:39348522-39348694 | Common:3; Rare:73 | ||||
| chr21:39380250-39380516 | Common:1; Rare:125 | ||||
| chr21:39445734-39445996 | Common:3; Rare:76 | ||||
| chr21:39451444-39451954 | Common:3; Rare:118 | ||||
| chr21:41426067-41426295 | Common:3; Rare:52 | ||||
| chr21:41879320-41879533 | Common:5; Rare:73 |